Core.X Flow Base

Dentsply DeTrey GmbH

Revision date : 2017-10-18

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GHS07
Health risk rating 4
Safety risk rating 1
Environmental risk rating 3

Note: Ingredients listed on restricted chemical lists

EC/CAS

3290-92-4

Name of the chemical

1,1,1-trimethylolpropane trimethacrylate

Concentration

N/A

General Information

Revision date

2017-10-18

Product name

Core.X Flow Base

1.2.1 Relevant identified uses

Core Build-Up Material

1.2.2. Uses advised against

No further relevant information available

Emergency telephone

+49-(0)7531-583-0 8 00 - 17 00 (GMT + 1 00

Icons in SDS

Company Information

company name

Dentsply DeTrey GmbH

e-mail address of the competent person responsible for the Safety Data Sheet

KonstanzDEU.info-sdb@dentsplysirona.com

GHS Information

Signal word

Warning

Hazard Codes

Hazard statements (CLP)

H315, H317, H319, H412

Hazard statements

Code

Statements

H315

Causes skin irritation

Section 2

CLP CLASSIFICATION

Skin Irrit. 2 H315 Causes skin irritation. Eye Irrit. 2 H319 Causes serious eye irritation. Skin Sens. 1 H317 May cause an allergic skin reaction. Aquatic Chronic 3 H412 Harmful to aquatic life with long lasting effects.

2.2 Label elements

Labelling according to Regulation (EC) No 1272/2008 The product is classified and labelled according to the CLP regulation.

Hazard pictograms

GHS07

Hazardous Ingredients

Urethane modified Bis-GMA dimethacrylate resin 2,2'-Ethylendioxydiethyldimethacrylat

Hazard statements

H315 Causes skin irritation. H319 Causes serious eye irritation. H317 May cause an allergic skin reaction. H412 Harmful to aquatic life with long lasting effects.

Precautionary statements

P261 Avoid breathing dust/fume/gas/mist/vapours/spray. P273 Avoid release to the environment. P280 Wear protective gloves / eye protection / face protection. P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P333+P313 If skin irritation or rash occurs: Get medical advice/attention. P501 Dispose of contents/container in accordance with local/regional/national/international regulations.

Additional information

As this product is a medical device in the meaning of Directive 93/42/EEC and intended for use by the end consumer and is applied in an invasive manner or body contact, it is exempt from the labelling requirements according to regulation 1272/2008.

PBT Substances

Not applicable

vPvB Substances

Not applicable *

SDS Library

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